4.6 Article

Photochemistry of 2-Propanol on Rutile TiO2(110)

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 126, Issue 8, Pages 3949-3956

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.1c09861

Keywords

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Funding

  1. National Key R&D Program of China [2018YFE0203002]
  2. National Natural Science Foundation of China [22173041, 22103033]
  3. Strategic Priority Research Program of Chinese Academy of Sciences [XDB17000000]
  4. Shenzhen Science and Technology Innovation Committee [JCYJ2019080914021660, ZDSYS20200421111001787]
  5. Guangdong Innovative & Entrepreneurial Research Team Program [2019ZT08L455, 2019JC01X091]
  6. International Partnership Program of Chinese Academy of Science [121421KYSB20170012]

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This study investigates the photodecomposition of 2-propanol on TiO2 surfaces and reveals the reaction behavior under different temperature and surface coverage conditions. The results indicate that higher temperature and lower 2-propanol surface coverage promote the formation of acetone.
2-Propanol is a typical volatile organic compound in air; the mechanistic studies of 2-propanol photodegradation on TiO2 are important for the development of efficient photocatalysts. Here, we report a systematic study of 2-propanol photodecomposition on rutile (R)-TiO2(110) using the temperature-programmed desorption method. Under 355 nm irradiation, the formation of acetone ((CH3)(2)CO) is clearly detected on reduced R-TiO2(110). The photoreactivity of molecular 2-propanol is much lower than that of 2-propoxy groups. As the surface temperature increases from 90 to 200 K, the yield of (CH3)(2)CO production is markedly enhanced by 7 times, which is most likely due to the shift of 2-propanol molecules into dissociated 2-propoxy groups at higher surface temperature. Furthermore, the additional steric hindrance from the two methyl groups of 2-propanol may also inhibit the formation of suitable structures for 2-propanol dissociation on R-TiO2(110) at high 2-propanol coverage, thus lowering the yield of (CH3)(2)CO formation. The results provide a fundamental insight into secondary alcohol photochemistry on TiO2.

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